1-(2,5-Dimethoxyphenyl)-5-(5,5-dimethyl-1,3-dioxan-2-yl)pentan-1-one, identified by its CAS number 898756-13-3, is a synthetic organic compound that belongs to the class of substituted phenyl ketones. This compound features a pentanone backbone, which is characterized by a five-carbon chain terminating in a ketone functional group. The presence of a 2,5-dimethoxyphenyl group indicates that the compound has two methoxy (-OCH₃) substituents on the aromatic ring, which can influence its electronic properties and reactivity. Additionally, the molecule contains a dioxane moiety, which contributes to its structural complexity and may affect its solubility and stability. Such compounds are often studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The specific characteristics, such as melting point, boiling point, and solubility, would depend on the compound's molecular interactions and the presence of functional groups, which can significantly influence its behavior in various chemical environments.

1-(2,5-dimethoxyphenyl)-5-(5,5-dimethyl-1,3-dioxan-2-yl)pentan-1-one

898756-13-3: 1-(2,5-Dimethoxyphenyl)-5-(5,5-dimethyl-1,3-dioxan-2-yl)pentan-1-one, identified by its CAS number 898756-13-3, is a synthetic organic compound that belongs to the class of substituted phenyl ketones. This compound features a pentanone backbone, which is characterized by a five-carbon chain terminating in a ketone functional group. The presence of a 2,5-dimethoxyphenyl group indicates that the compound has two methoxy (-OCH₃) substituents on the aromatic ring, which can influence its electronic properties and reactivity. Additionally, the molecule contains a dioxane moiety, which contributes to its structural complexity and may affect its solubility and stability. Such compounds are often studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The specific characteristics, such as melting point, boiling point, and solubility, would depend on the compound's molecular interactions and the presence of functional groups, which can significantly influence its behavior in various chemical environments.

CAS 898756-13-3

1-(2,5-dimethoxyphenyl)-5-(5,5-dimethyl-1,3-dioxan-2-yl)pentan-1-one

2′,5′-dimethoxy-5-(5,5-dimethyl-1,3-dioxan-2-yl)valerophenone

Ref: 10-F208416